{"created":"2023-05-15T12:35:14.797706+00:00","id":4071,"links":{},"metadata":{"_buckets":{"deposit":"db373531-a06c-438a-b5c4-959e5acc02cd"},"_deposit":{"created_by":3,"id":"4071","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"4071"},"status":"published"},"_oai":{"id":"oai:nitech.repo.nii.ac.jp:00004071","sets":["31"]},"author_link":["7387","11927","11929","10237"],"item_10001_biblio_info_28":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"1991-01-01","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"5","bibliographicPageEnd":"1234","bibliographicPageStart":"1231","bibliographicVolumeNumber":"1991","bibliographic_titles":[{"bibliographic_title":"Journal of the Chemical Society. Perkin transactions 1"}]}]},"item_10001_description_36":{"attribute_name":"内容記述","attribute_value_mlt":[{"subitem_description":"Treatment of diphenyl diselenide and tributylphosphine with aqueous NaOH was found to be a good method  for the generation of phenyl  selenide ion. A variety of 2-halogeno-1,4-naphthoquinones and halogenoquinolinequinones were efficiently converted into the corresponding seleno compounds. Selenenylation of 2,3-dichloro-1,4-naphthoquinone gave 2,3-bis(phenylseleno)-1,4-naphthoquinone. The reaction of 2-bromo-1,4-napthoquinone afforded 2,3-bis(phenylseleno) naphthoquinone in significant yield, in addition to 2-(phenylseleno) naphthoquinone as a major product. Formation of the diseleno compound was minimized when the reaction was carried out under completely oxygen-free conditions. The reaction mechanism of this selenenylation  is discussed.","subitem_description_type":"Other"}]},"item_10001_description_38":{"attribute_name":"フォーマット","attribute_value_mlt":[{"subitem_description":"application/pdf","subitem_description_type":"Other"}]},"item_10001_full_name_27":{"attribute_name":"著者別名","attribute_value_mlt":[{"nameIdentifiers":[{}],"names":[{"name":"融, 健"}]}]},"item_10001_publisher_29":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"Royal Society of Chemistry"}]},"item_10001_relation_34":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_name":[{"subitem_relation_name_text":"10.1039/P19910001231"}],"subitem_relation_type":"isIdenticalTo","subitem_relation_type_id":{"subitem_relation_type_id_text":"http://dx.doi.org/10.1039/P19910001231","subitem_relation_type_select":"DOI"}}]},"item_10001_source_id_30":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"14727781","subitem_source_identifier_type":"ISSN"}]},"item_10001_source_id_32":{"attribute_name":"書誌レコードID（NCID）","attribute_value_mlt":[{"subitem_source_identifier":"AA11413675","subitem_source_identifier_type":"NCID"}]},"item_10001_version_type_33":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Sakakibara, Makoto","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Watanabe, Yoshihiko","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Toru, Takeshi","creatorNameLang":"en"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Ueno, Yoshio","creatorNameLang":"en"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2017-01-23"}],"displaytype":"detail","filename":"JCSP 1991_1231.pdf","filesize":[{"value":"537.8 kB"}],"format":"application/pdf","license_note":"J. CHEM. SOC. PERKIN TRANS. 1 1991 , 1231-1234 -Reproduced by permission of The Royal Society of Chemistry (RSC)","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"本文_fulltext","url":"https://nitech.repo.nii.ac.jp/record/4071/files/JCSP 1991_1231.pdf"},"version_id":"3a94d42a-1d08-42e9-85ea-6f9d739c79e5"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"eng"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"New selenenylation method. Synthesis of selenonaphthoquinones and selenoquinolinequinones mediated by phenyl selenide ion","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"New selenenylation method. Synthesis of selenonaphthoquinones and selenoquinolinequinones mediated by phenyl selenide ion","subitem_title_language":"en"}]},"item_type_id":"10001","owner":"3","path":["31"],"pubdate":{"attribute_name":"公開日","attribute_value":"2012-11-06"},"publish_date":"2012-11-06","publish_status":"0","recid":"4071","relation_version_is_last":true,"title":["New selenenylation method. Synthesis of selenonaphthoquinones and selenoquinolinequinones mediated by phenyl selenide ion"],"weko_creator_id":"3","weko_shared_id":-1},"updated":"2023-05-16T14:52:52.807624+00:00"}